Chloromethyl Methyl Ether → 4-Bromo-2-methoxy-3-(methoxymethoxy)phenol

HRID 2171063Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2171063
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([O:9][CH3:10])[C:3]=1[OH:11].C(=O)([O-])[O-].[K+].[K+].[CH3:18][O:19][CH2:20]Cl>CC(C)=O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([O:9][CH3:10])[C:3]=1[O:11][CH2:18][O:19][CH3:20]

Komponenten

5

Edukt 3

HCID 7864Chloromethyl Methyl EtherHCID 11430Potassium CarbonateHCID 674653914-Bromo-2-methoxybenzene-1,3-diol

Produkt 1

HCID 674654874-Bromo-2-methoxy-3-(methoxymethoxy)phenolAusbeute 46,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 180AcetoneLösungsmittel

Versuchsvorschrift

To a stirring solution of 4-bromo-2-methoxybenzene-1,3-diol (4.5 g, 20.54 mmol) in acetone (40 mL) at 0° C. was added potassium carbonate (2.83 g, 20.54 mmol) and methoxymethyl chloride (1.32 mg, 16.43 mmol) and the resultant reaction mixture was stirred at RT for 7 h. The reaction mixture was quenched with ice-cold water, filtered and the filtrate was concentrated under reduced pressure. Purification of the residue by column chromatography (silica gel, 0-10% ethyl acetate in pet ether) afforded 4-Bromo-2-methoxy-3-(methoxymethoxy)phenol as a liquid (2 g, 37%).

Aufarbeitung

  1. customthe resultant reaction mixture
  2. customThe reaction mixture was quenched with ice-cold water
  3. filtrationfiltered
  4. concentrationthe filtrate was concentrated under reduced pressure
  5. customPurification of the residue by column chromatography (silica gel, 0-10% ethyl acetate in pet ether)

Quellen und Nachweise

ORD-Eintrag
ord-61f8b00f4f3649d095d194545bc0d955
Quelldatensatz
uspto-grants-2015_06
Patentnummer
US09051290B2

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